Abstract: A gas sensor includes a first electrode, a gas detecting layer disposed on the first electrode, and an electric-conduction enhanced electrode unit being electrically connected to the first electrode and the gas detecting layer. The electric-conduction enhanced electrode unit includes an electric-conduction enhancing layer and a second electrode electrically connected to the electric-conduction enhancing layer. The electric-conduction enhancing layer is electrically connected to the gas detecting layer and is made of an electrically conductive organic material.

Abstract: The present invention provides a fabrication method of a negative electrode for a secondary battery, including: (a) heating a slurry composition for a negative electrode containing a negative electrode active material, a binder, and a solvent to a temperature lower than a boiling point (Tb) of the solvent; (b) applying the heated slurry composition for a negative electrode onto a current collector; and (c) cooling the applied slurry composition for a negative electrode.

Abstract: A nonaqueous electrolyte secondary battery includes a positive electrode. The positive electrode includes a positive electrode active material layer. The positive electrode active material layer includes a first layer and a second layer. The first layer includes a first particle group. The second layer includes a mixture of a second particle group and a third particle group. The first particle group consists of a plurality of first positive electrode active material particles. The second particle group consists of a plurality of second positive electrode active material particles. The third particle group consists of a plurality of third positive electrode active material particles. Each of the first positive electrode active material particles and the third positive electrode active material particles independently includes 1 to 10 single-particles. Each of the second positive electrode active material particles includes secondary particles obtained by aggregation of 50 or more primary particles.

Abstract: The present invention provides a fabrication method of a multilayer electrode for a secondary battery including: (a) preparing two or more electrode slurries each containing an electrode active material, a binder, and a solvent and heating at least one electrode slurry selected from the prepared two or more electrode slurries to a temperature lower than a boiling point (Tb) of the solvent contained in the selected electrode slurry; (b) coating the two or more electrode slurries on a current collector; and (c) cooling the coated two or more electrode slurries.

Abstract: Provided is a method for producing an electrode active material capable of forming a non-aqueous secondary battery with superior durability and output characteristics. The method for producing an electrode active material for a non-aqueous secondary battery includes contacting a carbon material containing at least one selected from the group consisting of graphene, a carbon nanotube and carbon black with a one-electron oxidant having an oxidation-reduction potential of 0.2 V or more and 1.9 V or less to obtain at least one modified carbon material, and contacting the at least one modified carbon material with alkali-metal-transition-metal composite oxide particles.

Abstract: One aspect of the present invention is an energy storage device including a positive electrode containing: first positive active material particles containing a metal element capable of forming a conductive metal oxide; and second positive active material particles not containing the metal element, in which the first positive active material particles include a nickel-cobalt-manganese-containing lithium-transition metal composite oxide containing lithium, nickel, cobalt, and manganese as constituent elements, and the first positive active material particles are larger in median diameter than the second positive active material particles.

Abstract: A continuous process for producing a material of a battery cell using a system having a mist generator, a drying chamber, one or more gas-solid separators and a reactor is provided. A mist generated from a liquid mixture of two or more metal precursor compounds in desired ratio is dried inside the drying chamber. Heated air or gas is served as the gas source for forming various gas-solid mixtures and as the energy source for reactions inside the drying chamber and the reactor. One or more gas-solid separators are used in the system to separate gas-solid mixtures from the drying chamber into solid particles mixed with the metal precursor compounds and continuously deliver the solid particles into the reactor for further reaction to obtain final solid material particles with desired crystal structure, particle size, and morphology.

Abstract: One of the objects of the present invention is to provide an electrode having an active material layer and an insulating layer formed on a current collector in which the insulating layer has sufficient adhesion and which can be manufactured without significantly changing the manufacturing process. The electrode comprises a current collector 110, an active material layer 111 formed on at least one surface of the current collector 110, and an insulating layer 112 formed on the surface of the active material layer 111. The active material layer 111 includes an active material and a first binder. The insulating layer 112 includes non-conductive particles and a second binder. An interfacial binder ratio, which is a ratio of amount of a binder existing in an interface region between the active material layer 111 and the insulating layer 112 per unit thickness of the interface region to amount of a binder existing in the active material layer 111 per unit thickness of the active material layer 111, is 85% or more.

Abstract: An electrode includes a current collector; a first active material layer including a first active material; and a second active material layer including a second active material; wherein the first active material layer is arranged between the current collector and the second active material layer. The first active material layer is formed on a surface of the current collector, and a particle size of 90% accumulative volume of the first active material is less than 40 ?m. The active material layer is used to ensure that the electrochemical device and the electronic device do not generate a short circuit when pressed by an external force, thereby ensuring the mechanical safety performance of the electrochemical device and the electronic device.

Abstract: A secondary battery includes a body including a solid electrolyte layer, and a positive electrode and a negative electrode disposed with the solid electrolyte layer interposed therebetween; and first and second external electrodes respectively disposed on one surface and the other surface of the body, opposite to the one surface, and respectively connected to the positive electrode and the negative electrode, wherein the positive electrode comprises a positive electrode active material layer and a first electrolytic mixing portion disposed at an interface of the positive electrode in contact with the solid electrolyte layer. The first electrolytic mixing portion is a mixture of a positive electrode active material and a liquid phase and/or gel phase electrolyte.

Abstract: Provided are a binder aqueous solution for a lithium-ion battery electrode, a slurry for a lithium-ion battery electrode, a lithium-ion battery electrode, and a lithium-ion battery. The binder aqueous solution for a lithium-ion battery electrode contains a water-soluble polymer (A). The water-soluble polymer (A) is a polymer of a monomer group containing, with respect to 100 mol % of the monomer group, 5 mol % to 80 mol % of a hydroxyl group-containing vinyl ether (a). In one embodiment, the monomer group contains 20 mol % to 95 mol % of a (meth)acrylamide group-containing compound (b).

Abstract: A positive electrode active material for a secondary battery including: a lithium complex transition metal oxide which contains nickel (Ni) and cobalt (Co), and contains at least one selected from the group consisting of manganese (Mn) and aluminum (Al); and a composite coating portion which is formed on a surface of the lithium complex transition metal oxide is provided. The lithium complex transition metal oxide has a nickel (Ni) content of 65 mol % or more with respect to the total transition metal content, and the composite coating portion contains cobalt (Co) and boron (B), and contains at least one selected from the group consisting of lanthanum (La), titanium (Ti), and aluminum (Al).

Abstract: Provided is a method of manufacturing a porous core-shell catalyst structure. The method of manufacturing a porous core-shell catalyst structure includes preparing a bulk metal oxide; providing a first reaction gas containing nitrogen to the bulk metal oxide to prepare an intermediate product containing a porous metal oxide; and providing a second reaction gas containing sulfur to the intermediate product to prepare a core-shell catalyst structure including a core formed of the porous metal oxide and a shell formed of metal sulfide.

Abstract: Making a positive electrode active material for lithium ion secondary batteries includes: weighting and mixing lithium carbonate and a compound containing respective metallic elements other than Li in a composition formula Li?NixCoyM21-x-y-zM2zO2+? so as to have a metallic constituent ratio of the formula to obtain a mixture, and firing the mixture to obtain a lithium composite compound. Performing, on the mixture, a first heat treatment at 200° C. to 400° C. for 0.5 to 5 hours to obtain a first precursor. A step of performing a heat treatment on the first precursor under an oxidizing atmosphere at 450° C. to 800° C. for 0.5 to 50 hours, and reacting 92 mass % or more of the lithium carbonate to obtain a second precursor, and a finishing step of performing a heat treatment on the second precursor under an oxidizing atmosphere at 755° C. to 900° C. for 0.5 to 50 hours to obtain the lithium composite compound.

Abstract: A stabilized lithium ion cathode material comprising a calcined manganese oxide powder wherein the manganese on a surface is MnPO4, comprises an manganese phosphate bond, or the phosphate is bonded to the surface of the cathode material.

Abstract: A lithium-ion secondary battery positive electrode active material complex, a lithium-ion secondary battery positive electrode, and a lithium-ion secondary battery using the lithium-ion secondary battery positive electrode containing the lithium-ion secondary battery positive electrode active material complex are provided so that a lithium-ion secondary battery having high output properties, excellent durability, and a high energy density can be attained. A positive electrode active material for a lithium-ion secondary battery contains a complex in which a surface of a first positive electrode active material made of a lithium transition metal complex oxide containing nickel is covered with a covering layer containing an olivine type second positive electrode active material on a surface of which carbon is carried and a carbon nanotube.

Abstract: A deployable manufacturing center (DMC) system includes a foundry module containing a metallurgical system configured to convert a raw material into an alloy powder, and an additive manufacturing (AM) module containing an additive manufacturing system configured to form the alloy powder into metal parts. The deployable manufacturing center (DMC) system can also include a machining module containing a machining system configured to machine the metal parts into machined metal parts, and a quality conformance (QC) module containing an inspection and evaluation system configured to inspect and evaluate the metal parts. A process for manufacturing metal parts includes the steps of providing the deployable manufacturing center (DMC) system; deploying the (DMC) system to a desired location; forming an alloy powder from a raw material using the deployable foundry module; and then forming the metal parts from the alloy powder using the additive manufacturing (AM) module.

Abstract: An electrode includes a current collector; a first active material layer including a first active material; and a second active material layer including a second active material; wherein the first active material layer is arranged between the current collector and the second active material layer. The first active material layer is formed on a surface of the current collector, and a particle size of 90% accumulative volume of the first active material is less than 40 ?m. The active material layer is used in the present application to ensure that the electrochemical device and the electronic device do not generate a short circuit when pressed by an external force, thereby ensuring the mechanical safety performance of the electrochemical device and the electronic device.

Abstract: The present invention relates to a transition metal nitride support, a method of manufacturing the same, a metal catalyst and a platinum-alloy catalyst including the transition metal nitride support, and manufacturing methods thereof. The manufactured transition metal support prevents corrosion of the support and aggregation of the platinum catalyst, thereby exhibiting high oxygen reduction catalytic activity. Also, strong metal-support interaction (SMSI) can be stabilized, thus improving the durability of the catalyst. The transition metal support includes large pores uniformly distributed therein, thereby increasing the amount of the catalyst supported and minimizing mass-transfer resistance in a membrane- electrode assembly, increasing the performance of a polymer electrolyte membrane fuel cell. The metal catalyst includes platinum particles loaded on the transition metal nitride support, thus exhibiting superior durability and activity.

Abstract: An object is to suppress electrochemical decomposition of an electrolyte solution and the like at a negative electrode in a lithium ion battery or a lithium ion capacitor; thus, irreversible capacity is reduced, cycle performance is improved, or operating temperature range is extended. A negative electrode for a power storage device including a negative electrode current collector, a negative electrode active material layer which is over the negative electrode current collector and includes a plurality of particles of a negative electrode active material, and a film covering pan of the negative electrode active material. The film has an insulating property and lithium ion conductivity.

Abstract: The invention provides a positive electrode active material for a lithium ion battery, comprising a lithium transition metal-based oxide powder, the powder comprising single crystal monolithic particles comprising Ni and Co and having a general formula Li1+a ((Niz (Ni1/2 Mn1/2)y Cox)1?kAk)1-a 02, wherein A is a dopant, ?0.02<a?0.06, 0.10?x?0.35, 0?z?0.90, x+y+z=1 and k?0.01, the particles having a cobalt concentration gradient wherein the particle surface has a higher Co content than the particle center.

Abstract: Provided herein is a method for preparing a surface modified cathode material for lithium-ion battery, wherein the cathode material comprises lithium multi-metal composite oxide particles capped with a thin film of an oxide of the metal, wherein the lithium multi-metal composite oxide is represented by Li1+zNixMnyCo1?x?yO2; and wherein z is from 0 to 0.2; x is from 0.35 to 0.8; y is from 0.1 to 0.45; and the metal is one or more elements selected from the group consisting of Fe, Mn, Al, Mg, Zn, Ti, La, Ce, Sn, Zr, Ru and combination thereof. The cathode material disclosed herein exhibits a high initial specific capacity from 150 mAh/g to 200 mAh/g, possesses good safety characteristics and shows impressive energy retention of about 91% after 1000 cycles.

Abstract: There is provided a positive electrode for nonaqueous electrolyte secondary batteries in which a decrease in the initial charge capacity can be suppressed even when a positive electrode exposed to the air is used. A positive electrode for a nonaqueous electrolyte secondary battery according to an aspect of the present invention contains a lithium transition metal composite oxide represented by general formula Li1+xMnaMbO2+c (in the formula, x, a, b, and c satisfy x+a+b=1, 0<x?0.2, 0.09?a, and ?0.1?c?0.1, and M is at least one element selected from the group consisting of transition metal elements other than Mn, alkali metal elements, alkaline-earth metal elements, group 12 elements, group 13 elements, and group 14 elements) and also contains tungsten oxide and a phosphate compound.

Abstract: The present invention provides a method for preparing a positive active material for a secondary lithium battery. The method includes the steps of: synthesizing an intermediate product of a core represented by formula LixMyN1-yO2-?A?; adding P source into the intermediate product to obtain a phosphate which does not contain lithium; and adding lithium source into the mixture of the phosphate and LixMyN1-yO2-?A? and sintering to obtain the positive active material for secondary lithium battery. The method for preparing a positive active material for a secondary lithium battery of the present invention has the following advantages: 1) the P source can be dispersed on the surface of the core more uniformly; 2) the coating layer can be bonded to the core more tightly; and 3) the positive active material has higher rate discharge performance.

Abstract: A slip composition includes an electromagnetic-absorbing, magnetic powder having a mean particle size of not more than about 6 microns, a glass or vitreous frit having a mean particle size of not more than about 6 microns, and a methyl alcohol vehicle. A method of making a slip composition void of clay and aluminum oxide, includes mixing a wet milled vitreous frit, a powdered magnetic material, and a methyl alcohol vehicle. The disclosed embodiment is particularly useful in making an electromagnetic wave absorption coating suitable for application to stainless steel and many nickel base alloys.

Abstract: A method of forming an electrode active material by reacting a metal fluoride and a reactant. The method includes a coating step and a comparatively low temperature annealing step. Also included is the electrode formed following the method.

Abstract: A method of producing a positive electrode active material for a non-aqueous electrolyte secondary battery, the method including: stirring core particles including a lithium-transition metal composite oxide represented by a formula: LiaNi1-x-y-zCoxM1yM2zO2 wherein 1.00?a?1.50, 0.00?x?0.50, 0.00?y?0.50, 0.00?z?0.02, x+y?0.70, M1 is at least one element selected from the group consisting of Mn and Al, and M2 is at least one element selected from the group consisting of Zr, W, Ti, Mg, Ta, Nb and Mo; mixing the core particles with a first solution containing a rare earth element and a second solution containing a fluorine-containing compound, each independently, by adding dropwise the first solution and the second solution as the core particles are being stirred until the amount of the rare earth element added reaches 0.02 mol % to 0.15 mol % based on the amount of the core particles and the amount of the elemental fluorine added reaches 0.07 mol % to 0.

Abstract: A method for manufacturing a base material 2 for a superconductive conductor which includes: a conductive bed layer forming process of forming a non-oriented bed layer 24 having conductivity on a substrate 10; and a biaxially oriented layer forming process of forming a biaxially oriented layer 26 on the bed layer 24.

Abstract: Provided are a cathode active material including lithium transition metal phosphate particles, wherein the lithium transition metal phosphate particles include a first secondary particle formed by agglomeration of two or more first primary particles, and a second secondary particle formed by agglomeration of two or more second primary particles in the first secondary particle, and a method of preparing the same. Since the cathode active material according to an embodiment of the present invention may include first primary particles and second primary particles having different average particle diameters, the exfoliation of the cathode active material from a cathode collector may be minimized and performance characteristics, such as high output characteristics and an increase in available capacity, of a secondary battery may be further improved. In addition, since the first secondary particles are porous, the secondary particles are collapsed and fractured due to rolling when used in a cathode.

Abstract: A method for producing a nickel-containing surface coating that is metallic and conductive is provided. The method includes contacting a surface of a substrate with a liquid composition that includes nickel oxide nanoparticles, and modifying the nickel oxide nanoparticles to produce a nickel-containing metallic and conductive surface coating on the surface of the substrate. Also provided are nickel-containing (e.g., NiO and Ni containing) surface coatings and methods for making a liquid composition that includes nickel oxide nanoparticles. The methods and compositions find use in a variety of different applications.

Abstract: EC film stacks and different layers within the EC film stacks are disclosed. Methods of manufacturing these layers are also disclosed. In one embodiment, an EC layer comprises nanostructured EC layer. These layers may be manufactured by various methods, including, including, but not limited to glancing, angle deposition, oblique angle deposition, electrophoresis, electrolyte deposition, and atomic layer deposition. The nanostructured EC layers have a high specific surface area, improved response times, and higher color efficiency.

Abstract: The present invention provides additive manufacturing methods of forming multilayer energy storage devices on a surface by formulating all components of the multilayer energy storage device into liquid compositions and: (1) applying a first liquid current collector composition above the surface to form a first current collector layer above the surface; (2) applying a first liquid electrode composition above the first current collector layer to form a first electrode layer above the first current collector layer; (3) applying a liquid electrically insulating composition above the first electrode layer to form an electrically insulating layer above the first electrode layer; (4) applying a second liquid electrode composition above the electrically insulating layer to form a second electrode layer above the electrically insulating layer; and (5) applying a second liquid current collector composition above the second electrode layer to form a second current collector layer above the second electrode layer.

Abstract: The invention relates to an electrode material. Said material is characterized in that it contains, as positive electrode active material, at least one sulphate of iron in the +II oxidation state and of alkali metal corresponding to the formula (Na1?aLib)xFey(SO4), (I) in which the subscripts a, b, x, y and z are chosen so as to ensure the electroneutrality of the compound, with 0?a?1, 0?b?1, 1?x?3, 1?y?2, 1?z?3, and 2?(2z?x)/y<3 so that at least one portion of the iron is in the +II oxidation state, with the exclusion of the compound Li2Fe2(SO4)3. It is of use in particular as a positive electrode material in an alkali metal ion battery.

Abstract: Disclosed are an electrode for secondary batteries including an electrode mixture coated on one surface or opposite surface of an electrode current collector, and a method of manufacturing the same. The electrode mixture includes an electrode mixture layer A, which is a portion close to a current collector, and an electrode mixture layer, which is a portion distant from a current collector. The electrode mixture layer A includes a mixture of two active materials, average diameters of which are different, and the electrode mixture layer B includes active materials, average diameters of which are the same.

Abstract: A quantum-dots containing multi-component inorganic oxide thin film is provided to include an amorphous inorganic oxide bulk region and a plurality of crystalline inorganic oxide regions, wherein the crystalline inorganic oxide regions are discontinuously formed to be surrounded by the amorphous inorganic oxide of the bulk region.

Abstract: To provide a surface modified lithium-containing composite oxide having excellent discharge capacity, volume capacity density, safety, durability for charge and discharge cycles, and high rate property. A surface modified lithium-containing composite oxide, comprising particles of a lithium-containing composite oxide having a predetermined composition and a lithium titanium composite oxide containing lithium, titanium and element Q (wherein Q is at least one element selected from the group consisting of B, Al, Sc, Y and In) contained in the surface layer of the particles, wherein the lithium titanium composite oxide is contained in the surface layer of the particles in a proportion of the total amount of titanium and element Q in the lithium titanium composite oxide contained in the surface layer to the lithium-containing composite oxide particles is from 0.01 to 2 mol %, and the lithium titanium composite oxide has a peak at a diffraction angle 2? within a range of 43.8±0.

Abstract: An alkaline, rechargeable electrochemical cell includes a pasted electrode structure in which a composition comprising a paste matrix component includes cobalt in an amount greater than 6 weight percent ranging up to 14 weight percent. The matrix may also include a rare earth such as yttrium. The composition further includes particles of nickel hydroxide dispersed in the matrix, and these particles include cobalt levels ranging from greater than 8 atomic percent up to 15 atomic percent. Cells incorporating these materials have good charging efficiency at elevated temperatures.

Abstract: A method for depositing a thin film of a coating material onto an electrically conductive particle surface via supercritical fluid deposition includes providing electrically conductive particles, providing a precursor of a coating material, dissolving the precursor of the coating material into a supercritical fluid solvent to form a supercritical solution of the precursor and subsequently exposing the conductive particles to the supercritical solution in a reactor under conditions at which supercritical fluid deposition of a thin film of the coating material onto surfaces of the conductive particles occurs.

Abstract: Some implementations provide a semiconductor device that includes a die, an under bump metallization (UBM) structure coupled to the die, and a barrier layer. The UBM structure has a first oxide property. The barrier layer has a second oxide property that is more resistant to oxide removal from a flux material than the first oxide property of the UBM structure. The barrier layer includes a top portion, a bottom portion and a side portion. The top portion is coupled to the UBM structure, and the side portion is substantially oxidized.

Abstract: This LaNiO3 thin film-forming composition includes: LaNiO3 precursors; and acetic acid, wherein a ratio of an amount of the LaNiO3 precursors to 100 mass % of an amount of the LaNiO3 thin film-forming composition is in a range of 1 mass % to 20 mass % in terms of oxides, and the composition further includes a stabilizer containing N-methyl formamide in an amount of more than 0 mol to 10 mol or less per 1 mol of the total amount of the LaNiO3 precursors in the composition.

Abstract: Provided herein are energy storage device cathodes with high capacity electrochemically active material including compounds that include iron, fluorine, sulfur, and optionally oxygen. Batteries with active materials including a compound of the formula FeFaSbOc exhibit high capacity, high specific energy, high average discharge voltage, and low hysteresis, even when discharged at high rates. Iron, fluorine, and sulfur-containing compounds may be ionically and electronically conductive.

Abstract: A precursor of a modified ternary material for a lithium ion battery positive material belongs to the technical field of application of lithium ion battery positive materials. A molecular formula of the precursor is: (Ni1/3Co1/3Mn1/3)(OH)2, and the precursor consists of three layers. An inner layer of the precursor is a ternary material with the Co content of more than ? and equal Ni and Mn content, and the molecular formula of the inner layer of the precursor is: (Ni1/3?xCo1/3+2xMn1/3?x(OH)2, where 0<x??. An outer layer of the precursor is a ternary material with the Co content of 0 to ? and equal Ni and Mn content, and the molecular formula of the outer layer of the precursor is: (Ni0.5?yCo2yMn0.5?y)(OH)2, where 0?y<?. An intermediate layer of the precursor is a concentration gradient composite material of the two materials of the inner layer and the outer layer of the precursor. The modified ternary material containing the precursor has the chemical formula of Li(Ni1/3CO1/3Mn1/3)O2.

Abstract: A method for improving the lithium cobalt oxide (LiCoO2) film (such as films in thin film batteries) morphology includes using oxygen (O2) and argon (Ar) gases during sputtering deposition of the LiCoO2 film. This may allow for the manufacturing of thicker LiCoO2 films. Such a method may also significantly reduce or eliminate cracking and obvious columnar structures within the resulting LiCoO2 film layer. Sputtering using a mixture of O2 and Ar also may produce a LiCoO2 film layer that requires lower annealing temperatures to reach good utilization and has higher lithium diffusion rates.

Abstract: The invention relates to a method for fabricating an electrode which includes coating of an aqueous ink over the whole or part of a current collector followed by drying of said ink. The aqueous ink is produced by acidification of an aqueous dispersion including an electrochemically active material having a titanium and lithium oxide base until a pH value comprised between 9.0±0.1 and 10.0±0.1 is obtained. The invention also relates to an aqueous ink for an electrode including an electrochemically active material having a titanium and lithium oxide base and having a pH between 9.0±0.1 and 10.0±0.1, preferably equal to 10±0.1.

Abstract: The rechargeable lithium battery of the present invention includes a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte. The positive active material includes a core and a coating layer formed on the core. The core is made of a material such as LiCo0.98M?0.02O2, and the coating layer is made of a material such as MxPyOz. The electrolyte solution includes a nitrile-based additive. The rechargeable lithium battery of the present invention shows higher cycle-life characteristics and longer continuous charging time at high temperature.

Abstract: The rechargeable lithium battery includes a positive electrode which includes a positive active material, a negative electrode, and an electrolyte which includes a non-aqueous organic solvent and a lithium salt. The positive active material includes a core including at least one of a compound represented by Formula 1 and a compound represented by Formula 2, and a surface-treatment layer which is formed on the core and includes a compound represented by Formula 3. The lithium salt includes LiPF6 and a lithium imide-based compound. LiaNibCocMndMeO2??(1) LihMn2MiO4??(2) M?xPyOz??(3) wherein each of M and M? is independently selected from the group consisting of an alkali metal, an alkaline-earth metal, a Group 13 element, a Group 14 element, a transition element, a rare earth element, and combinations thereof, 0.95?a?1.1, 0?b?0.999, 0?c?0.999, 0?d?0.999, 0.001?e?0.2, 0.95?h?1.1, 0.001?i?0.2, 1?y?4, 0?y?7, and 2?z?30.

Abstract: A LaNiO3 thin film having extremely few voids is uniformly formed. Provided is a LaNiO3 thin film-forming composition for forming a LaNiO3 thin film. It includes: a LaNiO3 precursor; a first organic solvent; a stabilizer; and a second organic solvent. The first organic solvent includes carboxylic acids, alcohols, esters, ketones, ethers, cycloalkanes, aromatic compounds, or tetrahydrofuran. The stabilizer includes ?-diketones, ?-ketones, ?-keto esters, oxyacids, diols, triols, carboxylic acids, alkanolamines, or polyvalent amines. The second organic solvent has a boiling point of 150° C. to 300° C. and a surface tension of 20 to 50 dyn/cm. The LaNiO3 precursor content is 1 to 20 mass % with respect to 100 mass % of the composition. The stabilizer content is 0 to 10 mol with respect to 1 mol of a total amount of the LaNiO3 precursors. The second organic solvent content is 5 to 20 mass % with respect to the composition.

Abstract: Provided is a continuous process for preparing a high quality and high performance iron electrode. The process comprises preparing a formulation comprising an iron active material and a binder and coating a continuous substrate material on a least one side with the formulation. The coated continuous substrate material is dried, compacted and blanked. A tab is then attached to the electrode.

Abstract: The present invention provides one with a novel coated iron electrode. Provided is an iron based electrode comprising a single layer conductive substrate coated on at least one side with a multilayered coating, with each coating layer comprising an iron active material, and preferably a binder. The coating is comprised of at least two layers. Each layer has at least a different porosity or composition than an adjacent layer. The iron based electrode is useful in alkaline rechargeable batteries, particularly as a negative electrode in a Ni—Fe battery.

Abstract: A positive electrode active material includes: a secondary particle obtained upon aggregation of a primary particle that is a lithium complex oxide particle in which at least nickel (Ni) and cobalt (Co) are solid-solved as transition metals, wherein an average composition of the whole of the secondary particle is represented by the following formula (1): LixCoyNizM1-y-zOb-aXa ??Formula (1) wherein an existent amount of cobalt (Co) becomes large from a center of the primary particle toward the surface thereof; and an existent amount of cobalt (Co) in the primary particle existing in the vicinity of the surface of the secondary particle is larger than an existent amount of cobalt (Co) in the primary particle existing in the vicinity of the center of the secondary particle.